THE EQUALIZER AIRWAY DEVICE— 510(k) K870501

Substantially Equivalent

Sleep Renewal, Inc.

FDA 510(k) clearance K870501 for THE EQUALIZER AIRWAY DEVICE, Substantially Equivalent on 1987-03-04. Applicant: Sleep Renewal, Inc..

Clearance details

Applicant: Sleep Renewal, Inc.
Product code: Code LQZ
Advisory panel: Dental
Date received: 1987-02-04
Decision date: 1987-03-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mobile, AL, US

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